Molecular genetic studies in atrial fibrillation

Ling Ping Lai, Jiunn Lee Lin, Shoei K.Stephen Huang

Research output: Contribution to journalReview article

14 Citations (Scopus)

Abstract

Atrial fibrillation is a complex disease. Its etiologies are diverse and genetic factors may also contribute to this disease. With the advent of modern molecular biology technology, it is now possible to explore the genetic components in the pathogenesis of atrial fibrillation. Past molecular genetic studies on atrial fibrillation in the literature can be divided into linkage analysis studies and association studies. The subjects for linkage analysis studies are pedigrees of probands with Mendelian hereditary atrial fibrillation. The first locus identified for autosomal dominant atrial fibrillation locates at 10q22-q24. However, the exact gene is still unknown. Another linkage analysis study in Chinese revealed that LQT1 gene (IKs α-subunit) was the responsible gene. A missense mutation in the I Ks α-subunit results in a gain of function, which is important in causing atrial fibrillation. The third known locus for familial atrial fibrillation locates at 6q14-16. The responsible gene remains still unknown. The other type of studies takes the case-control design (association studies) and the subjects have multigenic atrial fibrillation. In a study in a Japanese population, it was reported that the angiotensin-converting enzyme insertion/deletion polymorphism was not associated with atrial fibrillation. On the other hand, researchers in Taiwan reported that a nonsynonymous single nucleotide polymorphism of the LQT5 gene (IKs β-subunit) is associated with atrial fibrillation. In summary, there is growing evidence showing that genetic factors are important in the pathogenesis of atrial fibrillation. We expect that more genes responsible for or contributing to atrial fibrillation will be identified in the future and these will elucidate the molecular mechanisms of atrial fibrillation.

Original languageEnglish
Pages (from-to)109-113
Number of pages5
JournalCardiology
Volume100
Issue number3
DOIs
Publication statusPublished - Dec 8 2003
Externally publishedYes

Fingerprint

Atrial Fibrillation
Molecular Biology
Genes
Peptidyl-Dipeptidase A
Missense Mutation
Pedigree
Taiwan
Single Nucleotide Polymorphism
Case-Control Studies
Research Personnel
Technology

Keywords

  • Atrial fibrillation
  • Genetics
  • Linkage analysis
  • Potassium channel

ASJC Scopus subject areas

  • Cardiology and Cardiovascular Medicine
  • Pharmacology (medical)

Cite this

Molecular genetic studies in atrial fibrillation. / Lai, Ling Ping; Lin, Jiunn Lee; Huang, Shoei K.Stephen.

In: Cardiology, Vol. 100, No. 3, 08.12.2003, p. 109-113.

Research output: Contribution to journalReview article

Lai, Ling Ping ; Lin, Jiunn Lee ; Huang, Shoei K.Stephen. / Molecular genetic studies in atrial fibrillation. In: Cardiology. 2003 ; Vol. 100, No. 3. pp. 109-113.
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